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Description

Much of USP-NF General Chapter <1231> Water for Pharmaceutical Purposes is devoted to instructing the water system owner/user of the issues associated with Microbial Control. Those issues are related to system design, choice of construction materials, routine operation, and routine unit operation maintenance, water delivery hose and connector care, and system sanitization, all intended to control or at least impede biofilm from getting a strong enough foothold in a water system to compromise its purification processes and/or contaminate the finished water used in the manufacture of pharmaceutical products. Attendees will learn about biofilm in water systems and how to successfully control it wherever it occurs, and why USP <1231> is a useful technical guide for microbial control in pharmaceutical water systems.

Miscellaneous

Certificate of Analysis (specimen)

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Product data sheet

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USP | United States Pharmacopeia

US Pharmacopeia Standards set a global benchmark, enabling efficient, reliable, and cost-effective development and quality control of pharmaceuticals.

Official USP Reference Standards are highly characterized physical specimens intended for quality control use when conducting assays and tests for medicines as described in the USP-NF. When you conduct tests and assays required by the USP-NF using the USP reference standards specified, the results can be considered conclusive.

As a USP-Authorized Distributor, we offer the following products and services:

  • USP Reference Standards
  • USP Pharmaceutical Analytical Impurities
  • USP Training and educational programs